瑞替普酶和阿昔单抗联合溶栓方案与标准瑞替普酶溶栓相比,纤维蛋白特异性增加,凝血酶激活减少。

S Szabo, D Etzel, R Ehlers, T Walter, S Kazmaier, U Helber, M E Beyer, H M Hoffmeister
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引用次数: 0

摘要

在接受溶栓治疗的急性心肌梗死患者中,血小板活化以及止血和纤溶系统的改变有利于早期梗死相关动脉再闭塞。我们研究了一种新的溶栓方案,即半剂量双剂量瑞替普酶(2 × 5 IU, 20例患者)联合阿昔单抗与全剂量瑞替普酶(2 × 10 IU, 18例患者)对急性st段抬高(心电图显示)心肌梗死患者的纤溶和止血系统的影响。半剂量雷替普酶联合阿昔单抗溶栓方案在体内引起较低的全体性纤溶酶血症和较低的凝血系统接触相的矛盾激活(以活化因子XII测量);较低的矛盾凝血酶激活/生成;并且纤维蛋白原分解的程度比雷替普酶方案要小。这些结果可以,至少部分地,解释在全球使用策略打开闭塞的冠状动脉V (GUSTO V)试验中,观察到的在入组后7天再梗死和再缺血发生率显著降低的联合组。
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Increased fibrin specificity and reduced paradoxical thrombin activation of the combined thrombolytic regimen with reteplase and abciximab versus standard reteplase thrombolysis.

In patients with acute myocardial infarction treated with thrombolytics, platelet activation as well as alterations of the hemostatic and fibrinolytic systems have been described favoring early infarct-related artery reocclusion. We investigated the effects of a newer thrombolytic regimen with half-dose double-bolus reteplase (2 x 5 IU, 20 patients) combined with abciximab versus full-dose reteplase (2 x 10 IU, 18 patients) on the fibrinolytic and the hemostatic system in patients with acute ST-segment elevation (in the electrocardiogram) myocardial infarction. The thrombolytic regimen with half-dose reteplase in combination with abciximab caused in vivo a lower systemic plasminemia and a lower paradoxical activation of the contact phase of the coagulation system (measured as activated factor XII); a lower paradoxical thrombin activation/generation; and a lesser extent of fibrinogen breakdown compared with the reteplase regimen. These results could be, at least in part, a possible explanation for the observed significantly lower rates of reinfarction until 7 days after enrollment and of recurrent ischemia in the combination group in the Global Use of Strategies to Open Occluded Coronary Arteries V (GUSTO V) trial.

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